{
    "disease_id": "DOID:4257", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007244", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007244", 
            "name": "cortical congenital hyperostosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007244", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007244", 
            "name": "infantile cortical hyperostosis"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:4257", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:4257", 
            "name": "cortical congenital hyperostosis"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:4257", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:4257", 
            "name": "infantile cortical hyperostosis"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:4257", 
        "description": "A bone inflammation disease that causes bone changes, soft tissue swelling and irritability in infants. The disease has been associated with COL1A1 gene. It has symptom soft-tissue swelling, has symptom bone lesions, and has symptom irritability.", 
        "resource": "Disease Ontology", 
        "id": "DOID:4257", 
        "name": "Caffey disease"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/4257#disease-associations", 
            "id": "4257", 
            "database": "Alliance of Genome Resources"
        }
    ]
}